(E)-3-(4-HYDROXYPHENYL)-1-(5-ISOPROPYLPYRAZIN-2-YL)PROP-2-EN-1-ONE

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Search structure


Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	VMYDEOJCEKPROI-VMPITWQZSA-N
Smiles	CC(C)c1cnc(cn1)C(=O)\C=C\c2ccc(O)cc2
InChI	InChI=1S/C16H16N2O2/c1-11(2)14-9-18-15(10-17-14)16(20)8-5-12-3-6-13(19)7-4-12/h3-11,19H,1-2H3/b8-5+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C16H16N2O2
Molecular Weight	268.31
AlogP	3.0
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	63.08
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	20.0

Assay Description	Organism	Bioactivity	Reference
Antifungal activity against Trichophyton mentagrophytes 445 after 120 hr by microdilution broth method	Trichophyton mentagrophytes	250000.0 nM
Antimycobacterial activity against Mycobacterium tuberculosis H37Rv ATCC 27294 at 12.5 ug/ml by microplate alamar blue assay relative to control	Mycobacterium tuberculosis H37Rv	72.0 %
Antifungal activity against Trichophyton mentagrophytes 445 after 72 hr by microdilution broth method	Trichophyton mentagrophytes	250000.0 nM
Inhibition of photosynthesis in Chlorella vulgaris chloroplast assessed as reduction of oxygen evolution rate after 4 hr by spectrophotometric analysis	Chlorella vulgaris	279000.0 nM
Inhibition of photosynthesis in Chlorella vulgaris assessed as reduction of chlorophyll production at 0.1 mM/l after 7 days by spectrophotometric analysis	Chlorella vulgaris	39.0 %
Inhibition of photosynthesis in Spinacia oleracea (spinach) chloroplast assessed as reduction of oxygen evolution rate after 4 hr by spectrophotometric analysis	Spinacia oleracea	315000.0 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2288596
PubChem	76309307

CONTENTS

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).